BRPI0616248A2 - compostos arilamidas substituÍdos por dioxazina e oxdiazina, processo para preparaÇço destes, e uso dos mesmos - Google Patents

compostos arilamidas substituÍdos por dioxazina e oxdiazina, processo para preparaÇço destes, e uso dos mesmos Download PDF

Info

Publication number: BRPI0616248A2
Authority: BR; Brazil
Prior art keywords: formula; compounds; alkyl; spp; haloalkyl
Prior art date: 2005-09-15

Application number

BRPI0616248-7A

Other languages

English (en)

Portuguese (pt)

Inventor

Achim Hense

Bernd Alig

Ruediger Fischer

Christian Funke

Ernst Rudolf Gesing

Olga Malsam

Mark Wilhelm Drewes

Christian Arnold

Peter Luemmen

Erich Sanwald

Bernd-Wieland Krueger

Original Assignee

Bayer Cropscience Ag

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2005-09-15

Filing date

2006-09-05

Publication date

2011-06-14

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=37442049&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=BRPI0616248(A2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

2006-09-05 Application filed by Bayer Cropscience Ag filed Critical Bayer Cropscience Ag

2011-06-14 Publication of BRPI0616248A2 publication Critical patent/BRPI0616248A2/pt

Links

150000001875 compounds Chemical class 0.000 title claims abstract description 78
238000002360 preparation method Methods 0.000 title claims abstract description 70
238000000034 method Methods 0.000 title claims abstract description 43
230000008569 process Effects 0.000 title claims abstract description 34
PPSZHCXTGRHULJ-UHFFFAOYSA-N dioxazine Chemical compound O1ON=CC=C1 PPSZHCXTGRHULJ-UHFFFAOYSA-N 0.000 title abstract description 13
244000045947 parasite Species 0.000 claims abstract description 9
238000004519 manufacturing process Methods 0.000 claims abstract description 4
-1 amino, aminoformyl Chemical group 0.000 claims description 105
239000013543 active substance Substances 0.000 claims description 54
239000002904 solvent Substances 0.000 claims description 36
239000001257 hydrogen Substances 0.000 claims description 35
229910052739 hydrogen Inorganic materials 0.000 claims description 35
229910052736 halogen Inorganic materials 0.000 claims description 30
150000002367 halogens Chemical class 0.000 claims description 30
150000002431 hydrogen Chemical group 0.000 claims description 30
239000000203 mixture Substances 0.000 claims description 27
125000004093 cyano group Chemical group *C#N 0.000 claims description 25
125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 24
125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 22
239000003085 diluting agent Substances 0.000 claims description 22
125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 20
239000003795 chemical substances by application Substances 0.000 claims description 19
125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 17
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 17
125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims description 15
125000000217 alkyl group Chemical group 0.000 claims description 15
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 14
125000001424 substituent group Chemical group 0.000 claims description 14
125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims description 13
125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 13
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 13
125000003545 alkoxy group Chemical group 0.000 claims description 12
239000000460 chlorine Substances 0.000 claims description 12
125000001841 imino group Chemical group [H]N=* 0.000 claims description 12
125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims description 11
125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 11
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 11
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 10
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 10
229910052801 chlorine Inorganic materials 0.000 claims description 10
229910052760 oxygen Inorganic materials 0.000 claims description 10
239000001301 oxygen Substances 0.000 claims description 10
239000011593 sulfur Substances 0.000 claims description 10
229910052717 sulfur Inorganic materials 0.000 claims description 10
125000004771 (C1-C4) haloalkylsulfinyl group Chemical group 0.000 claims description 8
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 8
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 8
229910052794 bromium Inorganic materials 0.000 claims description 8
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 8
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 8
125000004414 alkyl thio group Chemical group 0.000 claims description 7
150000003839 salts Chemical class 0.000 claims description 7
125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims description 6
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
244000000054 animal parasite Species 0.000 claims description 5
230000009261 transgenic effect Effects 0.000 claims description 5
150000001491 aromatic compounds Chemical class 0.000 claims description 4
239000003153 chemical reaction reagent Substances 0.000 claims description 4
239000003638 chemical reducing agent Substances 0.000 claims description 4
230000002140 halogenating effect Effects 0.000 claims description 4
125000001072 heteroaryl group Chemical group 0.000 claims description 4
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 3
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 3
150000001204 N-oxides Chemical class 0.000 claims description 3
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 3
125000001188 haloalkyl group Chemical group 0.000 claims description 3
125000004441 haloalkylsulfonyl group Chemical group 0.000 claims description 3
125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims description 2
230000003213 activating effect Effects 0.000 claims description 2
238000006482 condensation reaction Methods 0.000 claims description 2
125000001153 fluoro group Chemical group F* 0.000 claims description 2
125000003630 glycyl group Chemical group [H]N([H])C([H])([H])C(*)=O 0.000 claims description 2
125000005347 halocycloalkyl group Chemical group 0.000 claims description 2
150000002390 heteroarenes Chemical class 0.000 claims description 2
229910017053 inorganic salt Inorganic materials 0.000 claims description 2
125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims description 2
125000004092 methylthiomethyl group Chemical group [H]C([H])([H])SC([H])([H])* 0.000 claims description 2
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 2
125000003226 pyrazolyl group Chemical group 0.000 claims description 2
125000000168 pyrrolyl group Chemical group 0.000 claims description 2
239000000575 pesticide Substances 0.000 claims 2
125000004758 (C1-C4) alkoxyimino group Chemical group 0.000 claims 1
125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims 1
125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 claims 1
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
239000002168 alkylating agent Substances 0.000 claims 1
229940100198 alkylating agent Drugs 0.000 claims 1
125000000262 haloalkenyl group Chemical group 0.000 claims 1
230000000361 pesticidal effect Effects 0.000 claims 1
239000000126 substance Substances 0.000 abstract description 18
239000013067 intermediate product Substances 0.000 abstract description 5
241000196324 Embryophyta Species 0.000 description 63
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RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 30
238000012360 testing method Methods 0.000 description 28
239000003995 emulsifying agent Substances 0.000 description 27
ZMXDDKWLCZADIW-UHFFFAOYSA-N dimethylformamide Substances CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 24
239000004480 active ingredient Substances 0.000 description 23
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 21
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 19
239000003112 inhibitor Substances 0.000 description 19
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 18
239000012141 concentrate Substances 0.000 description 18
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 15
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
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230000000694 effects Effects 0.000 description 14
241001124076 Aphididae Species 0.000 description 13
238000009472 formulation Methods 0.000 description 13
239000000047 product Substances 0.000 description 13
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 12
241001465754 Metazoa Species 0.000 description 12
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 12
235000002017 Zea mays subsp mays Nutrition 0.000 description 11
235000019441 ethanol Nutrition 0.000 description 11
241000219146 Gossypium Species 0.000 description 10
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239000002253 acid Substances 0.000 description 9
238000006243 chemical reaction Methods 0.000 description 9
239000007858 starting material Substances 0.000 description 9
241000238631 Hexapoda Species 0.000 description 8
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 8
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
150000001448 anilines Chemical class 0.000 description 8
239000002917 insecticide Substances 0.000 description 8
KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 7
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 7
150000003254 radicals Chemical class 0.000 description 7
241000894007 species Species 0.000 description 7
241000238876 Acari Species 0.000 description 6
240000007124 Brassica oleracea Species 0.000 description 6
235000010469 Glycine max Nutrition 0.000 description 6
244000068988 Glycine max Species 0.000 description 6
241000721621 Myzus persicae Species 0.000 description 6
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 6
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 6
125000002877 alkyl aryl group Chemical group 0.000 description 6
230000015572 biosynthetic process Effects 0.000 description 6
235000005822 corn Nutrition 0.000 description 6
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 6
239000000975 dye Substances 0.000 description 6
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 6
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239000004009 herbicide Substances 0.000 description 6
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235000011152 sodium sulphate Nutrition 0.000 description 6
239000007921 spray Substances 0.000 description 6
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WWWTWPXKLJTKPM-UHFFFAOYSA-N 2-aminooxyethanol Chemical class NOCCO WWWTWPXKLJTKPM-UHFFFAOYSA-N 0.000 description 5
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125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 5
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239000011737 fluorine Substances 0.000 description 4
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INISTDXBRIBGOC-XMMISQBUSA-N tau-fluvalinate Chemical compound N([C@H](C(C)C)C(=O)OC(C#N)C=1C=C(OC=2C=CC=CC=2)C=CC=1)C1=CC=C(C(F)(F)F)C=C1Cl INISTDXBRIBGOC-XMMISQBUSA-N 0.000 description 1
AWYOMXWDGWUJHS-UHFFFAOYSA-N tebupirimfos Chemical compound CCOP(=S)(OC(C)C)OC1=CN=C(C(C)(C)C)N=C1 AWYOMXWDGWUJHS-UHFFFAOYSA-N 0.000 description 1
229950004921 temefos Drugs 0.000 description 1
WWJZWCUNLNYYAU-UHFFFAOYSA-N temephos Chemical compound C1=CC(OP(=S)(OC)OC)=CC=C1SC1=CC=C(OP(=S)(OC)OC)C=C1 WWJZWCUNLNYYAU-UHFFFAOYSA-N 0.000 description 1
DOMXUEMWDBAQBQ-WEVVVXLNSA-N terbinafine Chemical compound C1=CC=C2C(CN(C\C=C\C#CC(C)(C)C)C)=CC=CC2=C1 DOMXUEMWDBAQBQ-WEVVVXLNSA-N 0.000 description 1
229960002722 terbinafine Drugs 0.000 description 1
IWVCMVBTMGNXQD-UHFFFAOYSA-N terramycin dehydrate Natural products C1=CC=C2C(O)(C)C3C(O)C4C(N(C)C)C(O)=C(C(N)=O)C(=O)C4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-UHFFFAOYSA-N 0.000 description 1
HVZJRWJGKQPSFL-UHFFFAOYSA-N tert-Amyl methyl ether Chemical compound CCC(C)(C)OC HVZJRWJGKQPSFL-UHFFFAOYSA-N 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 1
UBCKGWBNUIFUST-YHYXMXQVSA-N tetrachlorvinphos Chemical compound COP(=O)(OC)O\C(=C/Cl)C1=CC(Cl)=C(Cl)C=C1Cl UBCKGWBNUIFUST-YHYXMXQVSA-N 0.000 description 1
MLGCXEBRWGEOQX-UHFFFAOYSA-N tetradifon Chemical compound C1=CC(Cl)=CC=C1S(=O)(=O)C1=CC(Cl)=C(Cl)C=C1Cl MLGCXEBRWGEOQX-UHFFFAOYSA-N 0.000 description 1
239000004308 thiabendazole Substances 0.000 description 1
235000010296 thiabendazole Nutrition 0.000 description 1
WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
229960004546 thiabendazole Drugs 0.000 description 1
BAKXBZPQTXCKRR-UHFFFAOYSA-N thiodicarb Chemical compound CSC(C)=NOC(=O)NSNC(=O)ON=C(C)SC BAKXBZPQTXCKRR-UHFFFAOYSA-N 0.000 description 1
OPASCBHCTNRLRM-UHFFFAOYSA-N thiometon Chemical compound CCSCCSP(=S)(OC)OC OPASCBHCTNRLRM-UHFFFAOYSA-N 0.000 description 1
QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical group COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
QSOHVSNIQHGFJU-UHFFFAOYSA-L thiosultap disodium Chemical compound [Na+].[Na+].[O-]S(=O)(=O)SCC(N(C)C)CSS([O-])(=O)=O QSOHVSNIQHGFJU-UHFFFAOYSA-L 0.000 description 1
229940074152 thuringiensin Drugs 0.000 description 1
238000003971 tillage Methods 0.000 description 1
210000001519 tissue Anatomy 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical compound COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-UHFFFAOYSA-N 0.000 description 1
HYVWIQDYBVKITD-UHFFFAOYSA-N tolylfluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=C(C)C=C1 HYVWIQDYBVKITD-UHFFFAOYSA-N 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
238000013519 translation Methods 0.000 description 1
125000004665 trialkylsilyl group Chemical group 0.000 description 1
AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 1
IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-UHFFFAOYSA-N 0.000 description 1
IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 description 1
ONCZDRURRATYFI-TVJDWZFNSA-N trifloxystrobin Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-TVJDWZFNSA-N 0.000 description 1
125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 1
125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
238000002211 ultraviolet spectrum Methods 0.000 description 1
229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
229940070710 valerate Drugs 0.000 description 1
NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
JARYYMUOCXVXNK-CSLFJTBJSA-N validamycin A Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-CSLFJTBJSA-N 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
BCEHBSKCWLPMDN-MGPLVRAMSA-N voriconazole Chemical compound C1([C@H](C)[C@](O)(CN2N=CN=C2)C=2C(=CC(F)=CC=2)F)=NC=NC=C1F BCEHBSKCWLPMDN-MGPLVRAMSA-N 0.000 description 1
229960004740 voriconazole Drugs 0.000 description 1
238000005406 washing Methods 0.000 description 1
239000001993 wax Substances 0.000 description 1
210000002268 wool Anatomy 0.000 description 1
WCJYTPVNMWIZCG-UHFFFAOYSA-N xylylcarb Chemical compound CNC(=O)OC1=CC=C(C)C(C)=C1 WCJYTPVNMWIZCG-UHFFFAOYSA-N 0.000 description 1
DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
FJBGIXKIXPUXBY-UHFFFAOYSA-N {2-[3-(4-chlorophenyl)propyl]-2,4,4-trimethyl-1,3-oxazolidin-3-yl}(imidazol-1-yl)methanone Chemical compound C1=CN=CN1C(=O)N1C(C)(C)COC1(C)CCCC1=CC=C(Cl)C=C1 FJBGIXKIXPUXBY-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/88—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with three ring hetero atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C259/00—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups
- C07C259/04—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids
- C07C259/10—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids having carbon atoms of hydroxamic groups bound to carbon atoms of six-membered aromatic rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C259/00—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups
- C07C259/12—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. N-hydroxyamidines
- C07C259/18—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. N-hydroxyamidines having carbon atoms of hydroxamidine groups bound to carbon atoms of six-membered aromatic rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D273/00—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D273/00—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00
- C07D273/01—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00 having one nitrogen atom
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D273/00—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00
- C07D273/02—Heterocyclic compounds containing rings having nitrogen and oxygen atoms as the only ring hetero atoms, not provided for by groups C07D261/00 - C07D271/00 having two nitrogen atoms and only one oxygen atom
- C07D273/04—Six-membered rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Plural Heterocyclic Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

BRPI0616248-7A 2005-09-15 2006-09-05 compostos arilamidas substituÍdos por dioxazina e oxdiazina, processo para preparaÇço destes, e uso dos mesmos BRPI0616248A2 (pt)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
DE102005044108A DE102005044108A1 (de)	2005-09-15	2005-09-15	Dioxazin- und Oxdiazin-substituierte Arylamide
DE102005044108.4		2005-09-15
PCT/EP2006/008637 WO2007031213A1 (fr)	2005-09-15	2006-09-05	Arylamides a substitution dioxazine et oxadiazine

Publications (1)

Publication Number	Publication Date
BRPI0616248A2 true BRPI0616248A2 (pt)	2011-06-14

Family

ID=37442049

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
BRPI0616248-7A BRPI0616248A2 (pt)	2005-09-15	2006-09-05	compostos arilamidas substituÍdos por dioxazina e oxdiazina, processo para preparaÇço destes, e uso dos mesmos

Country Status (12)

Country	Link
US (2)	US8062995B2 (fr)
EP (1)	EP1926728B1 (fr)
JP (1)	JP5124461B2 (fr)
KR (1)	KR101410281B1 (fr)
CN (1)	CN101287731B (fr)
AR (1)	AR056196A1 (fr)
AU (1)	AU2006291708A1 (fr)
BR (1)	BRPI0616248A2 (fr)
DE (1)	DE102005044108A1 (fr)
ES (1)	ES2629081T3 (fr)
TW (1)	TW200804361A (fr)
WO (1)	WO2007031213A1 (fr)

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EP2014658A1 (fr) *	2007-06-19	2009-01-14	Bayer CropScience AG	Dérivé de nicotinamide et son procédé de fabrication
EP2009001A1 (fr) *	2007-06-19	2008-12-31	Bayer CropScience AG	Procédé destiné à la fabrication de dérivés de dioxazine
BR112013000925A2 (pt)	2010-07-15	2020-12-01	Bayer Intellectual Property Gmbh	compostos heterocíclicos como pesticidas
IN2014CN03469A (fr) *	2011-11-21	2015-07-03	Basf Se
CN104031037B (zh) *	2014-06-23	2017-01-18	南京工业大学	一种含1，3，4‑噁二唑结构的甲酰苯胺类化合物及其制备方法与应用
CN104370899A (zh) *	2014-10-23	2015-02-25	南京工业大学	一种含1,2,4-噁二唑结构的甲酰苯胺类化合物及其制备方法与应用
US9802927B2 (en)	2015-06-10	2017-10-31	Denali Therapeutics, Inc.	Oxadiazine compounds and methods of use thereof
CN107987068A (zh) *	2017-12-08	2018-05-04	青岛清原化合物有限公司	一种二噁嗪衍生物及其制备方法、除草组合物和应用
CN108250156B (zh) *	2018-01-29	2021-07-09	华南农业大学	一种肉桂酸噁二嗪衍生物及其制备方法和应用
AR117461A1 (es) *	2018-12-20	2021-08-04	Bayer Ag	Compuestos de heterociclil piridazina como fungicidas
KR20230024343A (ko) *	2020-06-10	2023-02-20	바이엘 악티엔게젤샤프트	살진균제로서의 아자비시클릴-치환된 헤테로사이클
JP7735329B2 (ja) *	2020-06-18	2025-09-08	バイエル、アクチエンゲゼルシャフト	新規殺菌剤としてのオキサジアジニルピリダジン
EP4167740A1 (fr) *	2020-06-18	2023-04-26	Bayer Aktiengesellschaft	Combinaisons de composés actifs
US20240067624A1 (en) *	2021-01-11	2024-02-29	Upl Limited	Process for preparation of insecticidal anthranilamides

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JPH029855A (ja)	1988-03-31	1990-01-12	Ishihara Sangyo Kaisha Ltd	置換ベンゼン誘導体、それらの製造方法及びそれらを含有する抗癌性組成物
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GB9930750D0 (en)	1999-12-29	2000-02-16	Novartis Ag	Organic compounds
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BR0209912A (pt)	2001-05-21	2004-04-06	Du Pont	Composto, método de controle de pragas invertebradas e composição para controle das mesmas
AR036872A1 (es)	2001-08-13	2004-10-13	Du Pont	Compuesto de antranilamida, composicion que lo comprende y metodo para controlar una plaga de invertebrados
CA2454298A1 (fr)	2001-08-13	2003-02-27	Gary David Annis	Nouveaux 1h-dihydropyrazoles substitues et leurs procedes de preparation et d'utilisation
TWI327566B (en)	2001-08-13	2010-07-21	Du Pont	Novel substituted ihydro 3-halo-1h-pyrazole-5-carboxylates,their preparation and use
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RU2004107485A (ru)	2001-08-15	2005-03-27	Е.И.Дюпон де Немур энд Компани (US)	Орто-гетероциклические замещенные ариламиды для борьбы с беспозвоночными вредителями
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JP2005132727A (ja) *	2003-10-28	2005-05-26	Hokko Chem Ind Co Ltd	ジオキサジン誘導体および殺虫、殺ダニ剤

2005
- 2005-09-15 DE DE102005044108A patent/DE102005044108A1/de not_active Withdrawn
2006
- 2006-09-05 WO PCT/EP2006/008637 patent/WO2007031213A1/fr not_active Ceased
- 2006-09-05 US US11/992,006 patent/US8062995B2/en not_active Expired - Fee Related
- 2006-09-05 EP EP06777166.7A patent/EP1926728B1/fr not_active Not-in-force
- 2006-09-05 JP JP2008530380A patent/JP5124461B2/ja not_active Expired - Fee Related
- 2006-09-05 KR KR1020087008210A patent/KR101410281B1/ko not_active Expired - Fee Related
- 2006-09-05 CN CN2006800340100A patent/CN101287731B/zh not_active Expired - Fee Related
- 2006-09-05 AU AU2006291708A patent/AU2006291708A1/en not_active Abandoned
- 2006-09-05 BR BRPI0616248-7A patent/BRPI0616248A2/pt active Search and Examination
- 2006-09-05 ES ES06777166.7T patent/ES2629081T3/es active Active
- 2006-09-13 AR ARP060103992A patent/AR056196A1/es unknown
- 2006-09-14 TW TW095133959A patent/TW200804361A/zh unknown
2011
- 2011-11-09 US US13/292,517 patent/US8486934B2/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
CN101287731B (zh)	2012-02-08
JP5124461B2 (ja)	2013-01-23
EP1926728A1 (fr)	2008-06-04
US20120058891A1 (en)	2012-03-08
KR20080046694A (ko)	2008-05-27
US20090143228A1 (en)	2009-06-04
AR056196A1 (es)	2007-09-26
AU2006291708A1 (en)	2007-03-22
CN101287731A (zh)	2008-10-15
WO2007031213A1 (fr)	2007-03-22
EP1926728B1 (fr)	2017-04-05
KR101410281B1 (ko)	2014-06-23
TW200804361A (en)	2008-01-16
US8486934B2 (en)	2013-07-16
ES2629081T3 (es)	2017-08-07
US8062995B2 (en)	2011-11-22
DE102005044108A1 (de)	2007-03-29
JP2009512629A (ja)	2009-03-26

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CN102971315B (zh)	2015-07-22	作为害虫防治剂的噻唑衍生物
ES2542341T3 (es)	2015-08-04	Compuestos de enaminocarbonilo sustituidos como insecticidas
BRPI0715419B1 (pt)	2017-08-01	N'-cyano-n-halogenoalquil-imidamide derivatives, its use, composition, as a process for combating pests
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